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      Is acetaminophen associated with a risk of Stevens-Johnson syndrome and toxic epidermal necrolysis? Analysis of the French Pharmacovigilance Database : Risk of Stevens-Johnson syndrome and toxic epidermal necrolysis with acetaminophen

      1 , 2 , 3 , 4 , 5 , The French Network of Regional Centres of Pharmacovigilance and the French Investigators for Adverse Skin Reactions to Drugs
      British Journal of Clinical Pharmacology
      Wiley

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          Abstract

          <div class="section"> <a class="named-anchor" id="bcp13445-sec-0001"> <!-- named anchor --> </a> <h5 class="section-title" id="d967761e310">Aim</h5> <p id="d967761e312">Stevens–Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare but severe mostly drug‐induced cutaneous reactions. Acetaminophen is an over‐the‐counter drug used worldwide to treat pain and reduce fever. In 2013, the US Food and Drug Administration informed the public that acetaminophen was associated with a rare risk of SJS/TEN. The aim of the present retrospective study was to analyse reports of acetaminophen as a possible suspect in the development of SJS/TEN from the French Pharmacovigilance Database (FPDB). </p> </div><div class="section"> <a class="named-anchor" id="bcp13445-sec-0002"> <!-- named anchor --> </a> <h5 class="section-title" id="d967761e315">Methods</h5> <p id="d967761e317">Cases of TEN/SJS with acetaminophen as a suspect drug registered in the FPDB, collected from January 2002 to December 2013, were analysed by an expert group. The algorithm of drug causality for epidermal necrolysis (ALDEN) was used as a reference tool for SJS/TEN to assess the causality of each suspect drug. </p> </div><div class="section"> <a class="named-anchor" id="bcp13445-sec-0003"> <!-- named anchor --> </a> <h5 class="section-title" id="d967761e320">Results</h5> <p id="d967761e322">After exclusion of 16 nonvalidated cases, 112 cases (47 TEN, 51 SJS, 14 SJS/TEN overlaps) involving 574 suspected drugs (5⋅1/case) were analysed. In 80 cases, the acetaminophen ALDEN score was inferior or equal to that of other drugs, associated with a higher suspicion for causality. In 32 cases, acetaminophen had the highest score but matched with a ‘very unlikely’ or ‘unlikely’ causality in 12 cases. For the 20 remaining cases with a ‘possible’ or ‘ probable’ causality, a protopathic or a confounding bias was likely in 14 cases. </p> </div><div class="section"> <a class="named-anchor" id="bcp13445-sec-0004"> <!-- named anchor --> </a> <h5 class="section-title" id="d967761e325">Conclusions</h5> <p id="d967761e327">After analysis of the French pharmacovigilance data using the ALDEN algorithm, we found no obvious SJS/TEN risk related to the use of acetaminophen in this large national series. </p> </div>

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          ALDEN, an algorithm for assessment of drug causality in Stevens-Johnson Syndrome and toxic epidermal necrolysis: comparison with case-control analysis.

          Epidermal necrolysis (EN)--either Stevens-Johnson syndrome (SJS) or toxic EN (TEN)--is a severe drug reaction. We constructed and evaluated a specific algorithm, algorithm of drug causality for EN (ALDEN), in order to improve the individual assessment of drug causality in EN. ALDEN causality scores were compared with those from the French pharmacovigilance method in 100 cases and the case-control results of the EuroSCAR study. Scores attributed by ALDEN segregated widely. ALDEN pointed to a "probable" or "very probable" causality in 69/100 cases as compared to 23/100 with the French method (P < 0.001). It scored "very unlikely" causality for 64% of medications vs. none with the French method. Results of ALDEN scores were strongly correlated with those of the EuroSCAR case-control analysis for drugs associated with EN (r = 0.90, P < 0.0001), with probable causality being reported in 218/329 exposures. ALDEN excluded causality in 321 drugs that the case-control analysis had described as "probably not associated" and in 22/233 drugs that had been described as inconclusive exposures. Being more sensitive than a general method, ALDEN, which correlates well with case-control analysis results, can be considered a reference tool in SJS/TEN.
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            Medications as risk factors of Stevens-Johnson syndrome and toxic epidermal necrolysis in children: a pooled analysis.

            The aim of this study was to determine the relation of medications to the risk of Stevens-Johnson syndrome and toxic epidermal necrolysis in children <15 years of age. We conducted a pooled analysis by using data from 2 multicenter international case-control studies: the severe cutaneous adverse reaction (SCAR) study and the multinational severe cutaneous adverse reaction (EuroSCAR) study conducted in France, Germany, Italy, Portugal, the Netherlands, Austria, and Israel. We selected case subjects aged <15 years, hospitalized for Stevens-Johnson syndrome, Stevens-Johnson syndrome/toxic epidermal necrolysis-overlap, or toxic epidermal necrolysis, and age-, gender-, and country-matched hospital controls. Pooled crude odds ratios were estimated and adjusted for confounding by multivariate methods when numbers permitted. Our study included 80 cases and 216 matched controls. Antiinfective sulfonamides, phenobarbital, carbamazepine, and lamotrigine were strongly associated with the risk of Stevens-Johnson syndrome or toxic epidermal necrolysis. Significant associations were highlighted in univariate analysis for valproic acid and nonsteroidal antiinflammatory drugs as a group and for acetaminophen (paracetamol) in multivariate analysis. We confirmed 4 previously highly suspected drug risk factors for Stevens-Johnson syndrome/toxic epidermal necrolysis in children: antiinfective sulfonamides, phenobarbital, carbamazepine, and lamotrigine. Among more unexpected risk factors, we suspect that acetaminophen (paracetamol) use increases the risk of Stevens-Johnson syndrome or toxic epidermal necrolysis.
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              Correlations Between Clinical Patterns and Causes of Erythema Multiforme Majus, Stevens-Johnson Syndrome, and Toxic Epidermal Necrolysis

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                Author and article information

                Journal
                British Journal of Clinical Pharmacology
                Br J Clin Pharmacol
                Wiley
                03065251
                February 2018
                February 2018
                November 10 2017
                : 84
                : 2
                : 331-338
                Affiliations
                [1 ]Centre Régional de Pharmacovigilance; Hôpitaux Universitaires Pitié-Salpêtrière Charles-Foix, AP-HP; 47-83, Boulevard de l'Hôpital 75651 Cedex 13 Paris France
                [2 ]Centre Régional de Pharmacovigilance; CHU - Hôpital Nord; Avenue Albert Raimond 42055 Cedex 02 Saint-Etienne France
                [3 ]Centre Régional de Pharmacovigilance Marseille - Provence - Corse; Hôpital Sainte-Marguerite, AP-HM; 270 Boulevard de Saint-Marguerite 13009 Cedex 9 Marseille France
                [4 ]Centre Régional de Pharmacovigilance; CHU Amiens Sud; 80054 Cedex 1 Amiens France
                [5 ]Centre Régional de Pharmacovigilance, CHU - Centre de Biologie, EA 4681 PEPRADE; Université d'Auvergne; 58 Rue Montalembert -BP 69 63003 Cedex 1 Clermont-Ferrand France
                Article
                10.1111/bcp.13445
                5777438
                28963996
                33446d22-6622-4ee6-aca2-932c56ffd1fa
                © 2017

                http://doi.wiley.com/10.1002/tdm_license_1.1

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